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6874009: Congenital keratoderma (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
12370013 Congenital keratoderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
808609014 Congenital keratoderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital keratoderma est un(e) (attribut) kératose false Inferred relationship Some
Congenital keratoderma est un(e) (attribut) Rough skin (finding) true Inferred relationship Some
Congenital keratoderma est défini par la manifestation de (attribut) Abnormal keratinisation false Inferred relationship Some
Congenital keratoderma morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 2
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital keratoderma est un(e) (attribut) Erythrokeratoderma true Inferred relationship Some
Congenital keratoderma est un(e) (attribut) Skin lesion false Inferred relationship Some
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital keratoderma survenue (attribut) congénital false Inferred relationship Some 3
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
Congenital keratoderma morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Congenital keratoderma survenue (attribut) congénital true Inferred relationship Some 4
Congenital keratoderma morphologie associée (attribut) Hyperkeratosis true Inferred relationship Some 4
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 4
Congenital keratoderma est un(e) (attribut) Keratoderma true Inferred relationship Some
Congenital keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital keratoderma survenue (attribut) congénital false Inferred relationship Some
Congenital keratoderma morphologie associée (attribut) Hyperkeratosis false Inferred relationship Some 1
Congenital keratoderma est un(e) (attribut) Congenital disease true Inferred relationship Some
Congenital keratoderma a pour interprétation (attribut) anormal true Inferred relationship Some 2
Congenital keratoderma interprète (attribut) Keratinization, function (observable entity) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Erythrokeratodermia variabilis est un(e) (attribut) True Congenital keratoderma Inferred relationship Some
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder) est un(e) (attribut) True Congenital keratoderma Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) True Congenital keratoderma Inferred relationship Some
Mutilating keratoderma est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Keratosis palmaris et plantaris est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Keratoderma areata est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Keratoderma with pachyonychia congenita est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) est un(e) (attribut) True Congenital keratoderma Inferred relationship Some
Keratoderma with mental retardation and spastic paraplegia est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Keratoderma punctata est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Diffuse palmoplantar keratoderma est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Congenital palmoplantar and perioral keratoderma of Olmsted est un(e) (attribut) False Congenital keratoderma Inferred relationship Some
Naxos disease est un(e) (attribut) False Congenital keratoderma Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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